Functional role of the C-terminus of voltage-gated sodium channel Na(v)1.8

FEBS Lett. 2004 Aug 13;572(1-3):256-60. doi: 10.1016/j.febslet.2004.07.047.

Abstract

Sodium channel Na(v)1.8 requires stronger depolarization than other sodium channels for activation and inactivation. The contribution of Na(v)1.8 C-terminus to this property was investigated by producing Na(v)1.8 and Na(v)1.4 chimeras and expressing them in ND7/23 cells. Current densities of the chimeras were significantly different than in parental channels, and the voltage-dependence of activation was depolarized in Na(v)1.4/1.8C compared to Na(v)1.4. Analysis of steady-state inactivation showed that only Na(v)1.8 and Na(v)1.4/1.8C currents demonstrate a non-inactivated fraction. Thus, the C-terminus of Na(v)1.8 contributes to regulation of channel density at the cell surface, modulates channel gating, and regulates the generation of sustained current.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Cell Line
  • Ganglia, Spinal
  • Humans
  • Kinetics
  • Membrane Potentials / physiology
  • NAV1.8 Voltage-Gated Sodium Channel
  • Neurons / physiology
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Proteins / metabolism
  • Sodium Channels / genetics
  • Sodium Channels / physiology*
  • Transfection

Substances

  • NAV1.8 Voltage-Gated Sodium Channel
  • Recombinant Fusion Proteins
  • Recombinant Proteins
  • SCN10A protein, human
  • Sodium Channels